DOI: https://doi.org/10.63345/ijrmp.org.v10.i6.3
Disha Patel
Vadodara, Gujarat, India
Abstract
Chronic pain remains a major public health challenge, often refractory to conventional treatments. Recently, plant-derived nanomedicines have emerged as promising candidates for managing chronic pain due to their potential to improve bioavailability, reduce side effects, and target specific tissues. This study investigates the pharmacokinetic properties and therapeutic efficacy of several plant-based nanoformulations in preclinical models of chronic pain. We synthesized and characterized nanoparticles loaded with active phytochemicals known for their analgesic properties. Pharmacokinetic parameters were determined following oral and intravenous administration in rodent models, with the area under the curve, half-life, and tissue distribution serving as key metrics. In parallel, the analgesic efficacy was evaluated using validated behavioral assays and pain scales, comparing treated groups to standard analgesic regimens. A survey of clinicians and patients regarding the perceived benefits and potential barriers to nanomedicine adoption was also conducted. Statistical analyses, including regression and survival analyses, were performed to ensure robust interpretation of the data. The findings suggest that plant-derived nanomedicines not only improve pharmacokinetic profiles but also provide enhanced pain relief with fewer side effects compared to traditional treatments. These promising results lay the groundwork for future clinical studies and indicate that nanotechnology may represent a significant advancement in the treatment of chronic pain.
Keywords
Nanomedicine; Chronic Pain; Pharmacokinetics; Plant-derived; Efficacy; Analgesia; Preclinical.
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